Siemering K R, Praszkier J, Pittard A J
Department of Microbiology, University of Melbourne, Parkville, Victoria, Australia.
J Bacteriol. 1994 May;176(9):2677-88. doi: 10.1128/jb.176.9.2677-2688.1994.
The replication frequency of the IncB miniplasmid pMU720 is dependent upon the expression of the repA gene. Binding of a small, highly structured, antisense RNA (RNA I) to its complementary target in the RepA mRNA (RNA II) inhibits repA expression and thus regulates replication. Analyses of binding of RNA I to RNA II indicated that the reaction consists of three major steps. The first step, initial kissing complex formation, involves base pairing between complementary sequences in the hairpin loops of RNA I and RNA II. The second step is facilitated by interior loop structures in the upper stems of RNA I and RNA II and involves intrastand melting and interstrand pairing of the upper stem regions to form an extended kissing complex. This complex was shown to be sufficient for inhibition of repA expression. The third step involves stabilization of the extended kissing complex by pairing between complementary single-stranded tail regions of RNA I and RNA II. Thus, the final product of RNA I-RNA II binding is not a full duplex between the two molecules.
IncB小质粒pMU720的复制频率取决于repA基因的表达。一种小的、高度结构化的反义RNA(RNA I)与其在RepA mRNA(RNA II)中的互补靶标结合,会抑制repA的表达,从而调节复制。对RNA I与RNA II结合的分析表明,该反应包括三个主要步骤。第一步,初始的“亲吻”复合体形成,涉及RNA I和RNA II发夹环中互补序列之间的碱基配对。第二步由RNA I和RNA II上部茎干中的内环结构促进,涉及上部茎干区域的链内解链和链间配对,以形成延伸的“亲吻”复合体。已证明该复合体足以抑制repA的表达。第三步涉及通过RNA I和RNA II互补单链尾部区域之间的配对来稳定延伸的“亲吻”复合体。因此,RNA I-RNA II结合的最终产物不是两个分子之间的完全双链体。